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. 2025 Apr 20;32(4):240.
doi: 10.3390/curroncol32040240.

Cost-Effectiveness Analysis of Contemporary Advanced Prostate Cancer Treatment Sequences

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Cost-Effectiveness Analysis of Contemporary Advanced Prostate Cancer Treatment Sequences

Valentyn Litvin et al. Curr Oncol. .

Abstract

There has been a proliferation of novel treatments for the management of advanced prostate cancer (PCa), including androgen receptor pathway inhibitors (ARPI). Although there are health economic analyses of novel PCa treatments, such as ARPIs for specific health states, there is a lack of sequential analyses. Our paper aims to fill this gap. We developed a Monte Carlo Markov model to simulate the management of advanced PCa to end-of-life. We modeled patients who begin in metastatic and nonmetastatic castration-sensitive PCa (mCSPC and nmCSPC), with risk stratification for mCSPC, progressing to metastatic castration-resistant PCa (mCRPC). Using current guidelines and recent literature, we simulated admissible treatment sequences over these states along a 15-year horizon. We report the best treatment sequences in terms of efficacy and cost-effectiveness. We find that the most cost-effective use of ARPIs is early in advanced PCa for a cost-effectiveness threshold (CET) of CAD 100K per QALY. For a CET of CAD 50K per QALY, early ARPI use is most cost-effective in mCSPC-starting patients but not nmCSPC-starting. We conclude that the most cost-effective way to use ARPIs is when patients first enter advanced PCa. The most cost-effective ARPI at current Canadian prices is abiraterone, mostly due to abiraterone's lower price level.

Keywords: androgen-receptor pathway inhibitor; cost-effectiveness; prostate cancer; treatment sequence.

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Conflict of interest statement

The authors declare no conflicts of interest.

Figures

Figure 1
Figure 1
State transition diagram.
Figure 2
Figure 2
Acceptability curves for (a) patients starting in nmCSPC, (b) patients starting in low-risk mCSPC, and (c) patients starting in high-risk mCSPC.
Figure 3
Figure 3
Tornado diagram examining sensitivity scenarios for (a) patients starting in nmCSPC, (b) patients starting in low-risk mCSPC, and (c) patients starting in high-risk mCSPC.

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References

    1. Wang L., Lu B., He M., Wang Y., Wang Z., Du L. Prostate Cancer Incidence and Mortality: Global Status and Temporal Trends in 89 Countries From 2000 to 2019. Front. Public Health. 2022;10:811044. doi: 10.3389/fpubh.2022.811044. - DOI - PMC - PubMed
    1. Freedland S.J., Luz M.d.A., De Giorgi U., Gleave M., Gotto G.T., Pieczonka C.M., Haas G.P., Kim C.-S., Ramirez-Backhaus M., Rannikko A., et al. Improved Outcomes with Enzalutamide in Biochemically Recurrent Prostate Cancer. N. Engl. J. Med. 2023;389:1453–1465. doi: 10.1056/NEJMoa2303974. - DOI - PubMed
    1. Chi K.N., Chowdhury S., Bjartell A., Chung B.H., Pereira de Santana Gomes A.J., Given A., Juárez A., Merseburger A.S., Özgüroğlu M., Uemura H., et al. Apalutamide in patients with metastatic castration-sensitive prostate cancer: Final survival analysis of the randomized, double-blind, phase III TITAN study. J. Clin. Oncol. 2021;39:2294–2303. doi: 10.1200/JCO.20.03488. - DOI - PubMed
    1. Fizazi K., Foulon S., Carles J., Roubaud G., McDermott R., Fléchon A., Tombal B., Supiot S., Berthold D., Ronchin P., et al. Abiraterone plus prednisone added to androgen deprivation therapy and docetaxel in de novo metastatic castration-sensitive prostate cancer (PEACE-1): A multicentre, open-label, randomised, phase 3 study with a 2×2 factorial design. Lancet. 2022;399:1695–1707. doi: 10.1016/S0140-6736(22)00367-1. - DOI - PubMed
    1. Hoyle A.P., Ali A., James N.D., Cook A., Parker C.C., de Bono J.S., Attard G., Chowdhury S., Cross W.R., Dearnaley D.P., et al. Abiraterone in “high-” and “low-risk” metastatic hormone-sensitive prostate cancer. Eur. Urol. 2019;76:719–728. doi: 10.1016/j.eururo.2019.08.006. - DOI - PubMed

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